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首页> 外文期刊>Cytopathology >Monitoring and evaluating the performance of the UK NHS Cervical Screening Programme: monitoring performance by using cytology outcomes adjusted for population characteristics.
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Monitoring and evaluating the performance of the UK NHS Cervical Screening Programme: monitoring performance by using cytology outcomes adjusted for population characteristics.

机译:监测和评估英国NHS子宫颈筛查计划的效果:通过使用针对人群特征调整的细胞学结果监测效果。

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Current quality assurance measures used in the NHS cervical screening programme (NHSCSP) include a review of laboratories with percentages of moderate/severe and borderline/mild smear results outside the 10th-90th percentiles. The method is limited by the fact that many of these outlier smear percentages may reflect laboratories covering populations with low or high risk and/or short or long average screening intervals. This paper outlines a new approach to aid the detection of outlier laboratories, by using data collected at the primary care trust (PCT) or health authority (HA) level and making allowances for population characteristics and screening interval. The setting is the NHSCSP in England using annual data provided by HAs. Data from the screening year 2000-01 is used to illustrate the methodology, although the methods can also be applied to data at the PCT level (now being collected for 2002-03 onwards). Percentages of smear results have been analysed against a series of explanatory variables using logistic regression models. These explanatory variables include Townsend deprivation index, uptake-corrected ethnic minority composition, a measure of screening interval, area type and region. An expected percentage of borderline/mild and moderate/severe smears is estimated from the models and an observed : predicted ratio (OPRmod/sev and OPRbord/mild) calculated. Low values are suggestive of relative undercalling and high values overcalling, after allowance for population characteristics. Analysis of data for 2000-01 showed that the OPRmod/sev for the 99 HAs varied from 0.68 to 1.44. Laboratories with low percentages of moderate/severe smears, but associated with PCTs or HAs with OPRmod/sev values closer to unity may not need to be investigated as their observed rates are consistent with predicted rates based on population characteristics. The method could also be directly applied to laboratories if further information on the population covered by each laboratory were routinely collected.
机译:NHS子宫颈筛查计划(NHSCSP)中使用的当前质量保证措施包括对实验室的审查,这些实验室的中/重度和临界/轻度涂片结果的百分比在10%至90%百分位之外。该方法受到以下事实的限制:许多这些异常涂片百分比可能反映了实验室覆盖了具有低风险或高风险和/或较短或较长的平均筛查间隔的人群。本文概述了一种新方法,该方法通过使用在初级保健信托(PCT)或卫生当局(HA)级别收集的数据并考虑人群特征和筛查间隔,来辅助检测异常实验室。设置为使用房委会提供的年度数据的英格兰NHSCSP。尽管也可以将这些方法应用于PCT级别的数据(现已从2002-03年开始收集),但是使用来自2000-01筛选年的数据来说明该方法。使用逻辑回归模型,针对一系列解释变量分析了涂片结果的百分比。这些解释性变量包括汤森(Townsend)剥夺指数,摄取校正的少数民族组成,筛查间隔,面积类型和区域的度量。从模型中估计边界/轻度和中度/重度涂片的预期百分比,并计算观察到的预测比率(OPRmod / sev和OPRbord /轻度)。在考虑到人口特征后,低值表示相对应销,高值则应覆盖。对2000年1月数据的分析表明,99个HA的OPRmod / sev在0.68至1.44之间变化。具有中等/重度涂片百分比低但与OPRmod / sev值更接近统一的PCT或HA的实验室可能不需要进行研究,因为它们的观察率与基于人群特征的预测率一致。如果常规收集有关每个实验室所覆盖人群的更多信息,则该方法也可以直接应用于实验室。

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